Skip to main content
●+254 119 023975 support@dnalabskenya.com
Patient Portal LoginB2B / Doctor Portal
DNA LabsKenya
Medical information Clinical review pending

Genetic Testing

AMELX Gene Amelogenesis Imperfecta Type 1E Genetic Test

Genetic test to identify mutations in the AMELX gene associated with Amelogenesis Imperfecta Type 1E, a condition affecting tooth enamel development.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

Ask a question
Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Blood sample (EDTA tube), extracted DNA, or a single drop of blood on an FTA card.
Results
Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required. A genetic counseling session prior to testing is recommended, especially if there is a known family history.
Test priceKSh 40,000

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the AMELX Gene Amelogenesis Imperfecta Type 1E Genetic Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

+254

Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

WhatsApp the claims team Call us
01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Individuals with suspected Amelogenesis Imperfecta.
  • ✓Family history of enamel defects or Amelogenesis Imperfecta.
  • ✓Patients with unexplained enamel hypoplasia or hypomineralization.
  • ✓Recurrent dental problems potentially linked to genetic factors.
  • ✓Prenatal diagnosis or carrier screening in affected families.
02

In plain language

What this test helps you understand

This test helps confirm a diagnosis of Amelogenesis Imperfecta Type 1E, identify the specific genetic mutation causing the condition, and provide information for genetic counseling and family planning.
This genetic test identifies mutations in the AMELX gene, which can cause Amelogenesis Imperfecta Type 1E, a disorder affecting the formation of tooth enamel. It uses next-generation sequencing (NGS) technology to analyze your DNA for specific changes in this gene. Understanding these genetic factors can provide insights into dental health issues and guide management strategies. This test is particularly relevant for individuals with a family history of enamel defects or those presenting with symptoms like discolored, pitted, or easily damaged teeth. Results are interpreted by genetic professionals, and discussing them with your healthcare provider is crucial for understanding their implications.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationNo specific patient preparation is required. A genetic counseling session prior to testing is recommended, especially if there is a known family history.
SampleBlood sample (EDTA tube), extracted DNA, or a single drop of blood on an FTA card.
MethodologyNext-Generation Sequencing (NGS) is used to detect mutations within the AMELX gene.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test specifically analyzes the AMELX gene for mutations associated with Amelogenesis Imperfecta Type 1E. It does not detect mutations in other genes that can cause similar conditions. Results may be inconclusive in rare cases. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

It is a genetic disorder affecting tooth enamel formation, leading to defects in the enamel's structure, appearance, and durability. Type 1E is specifically linked to mutations in the AMELX gene.
Individuals with symptoms of enamel defects (e.g., discolored, pitted, easily broken teeth) or a family history of Amelogenesis Imperfecta should consider this test.
A positive result indicates that a mutation in the AMELX gene associated with Amelogenesis Imperfecta Type 1E has been identified. Discuss the implications with your doctor.
A blood sample, extracted DNA, or a single drop of blood on an FTA card is required for the test.
Confirm with the laboratory before booking.
Yes, genetic counseling is recommended before testing to understand the test's implications and after receiving results to discuss their meaning.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

Explore partnerships
09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

Keep exploring

Related tests

View all tests →

Beta CTx Beta Crosslaps Collagen Type 1 C-Telopeptide Test

The Beta CTx test measures bone resorption markers to help assess bone health and osteoporosis risk.

Learn more →

Bcell Rearrangement Detection Test

The Bcell Rearrangement Detection Test helps diagnose leukemia by identifying genetic changes in B cells. It's a key tool for hematologists and oncologists.

Learn more →

Dpd Gene Mutations 5Fu Toxicity Detection Test

This genetic test identifies mutations in the DPD gene, helping predict the risk of severe side effects from the chemotherapy drug 5-fluorouracil (5FU).

Learn more →

Ganciclovir Resistance Detection Test

This test checks for genetic changes in the cytomegalovirus (CMV) that may make it resistant to the antiviral medication Ganciclovir. It helps guide treatment decisions, especially for patients with weakened immune systems.

Learn more →
Chat on WhatsApp